CN1638635A - Fungicidal mixtures based on prothioconazole and containing an insecticide - Google Patents

Fungicidal mixtures based on prothioconazole and containing an insecticide Download PDF

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Publication number
CN1638635A
CN1638635A CNA038054299A CN03805429A CN1638635A CN 1638635 A CN1638635 A CN 1638635A CN A038054299 A CNA038054299 A CN A038054299A CN 03805429 A CN03805429 A CN 03805429A CN 1638635 A CN1638635 A CN 1638635A
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formula
compound
prothioconazole
iii
mixture
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CN100393214C (en
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E·安莫曼
R·施蒂尔勒
G·洛伦兹
S·斯特瑞斯曼
K·谢尔伯格
V·J·斯帕达福拉
T·克里斯滕
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BASF SE
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    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/647—Triazoles; Hydrogenated triazoles
    • A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles

Abstract

The invention relates to a fungicidal mixture containing (1) 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2, 4-dihydro-[1,2,4]-triazole-3-thione (prothioconazole) of formula (I), or the salts or adducts thereof and at least one insecticide, selected from (2) fipronil of formula (II), or chloropyrifos of formula (III), or (4) thiamethoxam of formula (IV) in a synergistically effective quantity.

Description

Based on Prothioconazole and contain the Fungicidal mixture of insecticide
The present invention relates to Fungicidal mixture, it comprises the following component of cooperative effective quantity:
(1) 2-[2-of formula I (1-chlorine cyclopropyl)-3-(2-chlorphenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazole-3-thioketones (Prothioconazole) or its salt or adduct:
Figure A0380542900041
Be selected from following insecticide with at least a:
(2) the sharp strength spy of formula II:
Figure A0380542900042
Or
(3) chlopyrifos of formula III:
Figure A0380542900043
Or
(4) the thiophene worm piperazine (Thiamethoxam) of formula IV:
Figure A0380542900044
In addition, the present invention relates to a kind of at least a mixture methods for fighting harmful mushrooms of using among Compound I and Compound I I, III or the IV, Compound I, II, III and IV preparation in such mixture purposes and the composition that comprises these mixtures.
Formula I compound, i.e. 2-[2-(1-chlorine cyclopropyl)-3-(2-chlorphenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazole-3-thioketones (Prothioconazole) is known by WO 96/16048.
WO 98/47367 discloses the many reactive compound combinations of Prothioconazole with a large amount of other Fungicidal compounds.
The sharp strength spy of formula II is described in Pest.Man. (agricultural chemicals handbook), and the 12nd edition (2000) are in the 413rd page.
The chlopyrifos of formula III also is known and is described among the DE-A-1 445 659.
At last, the thiophene worm piperazine of formula IV is known equally and is described among the EP-A 580553.
The purpose of this invention is to provide harmful fungoid is had the mixture (Synergistic mixture) that the total amount of application of improved activity and reactive compound reduces, to reduce rate of application and to improve the activity profile of known compound I, II, III and IV.
We find that this purpose is by the mixture realization of the Prothioconazole that limited of beginning with at least a insecticide.In addition, we find to use simultaneously, promptly use together or separately administered compound I and at least a other Compound I I, III or IV, or at least a harmful fungoid preventive and therapeutic effect that provides among administered compound I and Compound I I, III or the IV is better than using may acting on of each compound separately successively.
The 2-[2-of formula I (1-chlorine cyclopropyl)-3-(2-chlorphenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazole-3-thioketones is known by WO 96-16048.This compound can following formula " thioketones " form exist:
Or exist with tautomerism " mercaptan " form of following formula:
For the sake of simplicity, only provide " thioketones " form in each case.
The sharp strength spy of formula II is described in Pest.Man., and the 12nd edition (2000), in the 413rd page:
Figure A0380542900062
The chlopyrifos of formula III is described among the DE-A-1 445 659:
Figure A0380542900063
The thiophene worm piperazine of formula IV is described among the EP-A-580 553:
Figure A0380542900064
Because their nitrogen-atoms is alkalescence, Compound I can form salt or adduct with inorganic or organic acid or with metal ion.
Representative examples of mineral pigments is halogen acids such as hydrofluoric acid, hydrochloric acid, hydrobromic acid and hydroiodic acid, carbonic acid, sulfuric acid, phosphoric acid and nitric acid.
Appropriate organic for example is a formic acid, carbonic acid and alkanoic acid, as acetate, trifluoroacetic acid, trichloroacetic acid and propionic acid, and also has glycolic acid, thiocyanic acid, lactic acid, succinic acid, citric acid, benzoic acid, cinnamic acid, oxalic acid, alkyl sulfonic acid (having the straight chain that has 1-20 carbon atom or the sulfonic acid of branched-alkyl), aryl sulfonic acid or aryl disulfonic (aromatic group such as phenyl and naphthyl, it has one or two sulfonic group), alkyl phosphonic acid (having the straight chain that has 1-20 carbon atom or the phosphonic acids of branched-alkyl), arylphosphonic acid or aryl di 2 ethylhexyl phosphonic acid (aromatic group such as phenyl and naphthyl, it has one or two phosphonyl group), wherein alkyl or aryl can have other substituting group, for example p-methyl benzenesulfonic acid, salicylic acid, Para-amino-salicylic acid, the 2-phenoxy benzoic acid, 2-acetoxy-benzoic acid etc.
Suitable metal ion is the ion of second major element especially, especially the ion of calcium and magnesium; The ion of third and fourth major element, especially aluminium, tin and plumbous ion; The ion of the ion of first to the 8th transition element, especially chromium, manganese, iron, cobalt, nickel, copper and zinc; And other ion.The ion of preferred especially period 4 transition element.Metal can exist by the various chemical valences that they may present.
Preferred Prothioconazole and sharp strength spy's mixture.
In addition, the mixture of also preferred Prothioconazole and chlopyrifos.
The mixture of also preferred Prothioconazole and thiophene worm piperazine.
Two kinds ternary mixture in the also preferred above-mentioned insecticide of Prothioeonazole.
When the preparation mixture, pure reactive compound I, II, III and the IV of preferred use, can be to the reactive compound that wherein adds other antagonism harmful fungoid or other insect such as insect, spider or nematode, or have the reactive compound or the fertilizer of herbicide effect or growth regulating effect.
At least a mixture among Compound I and Compound I I, III and the IV, perhaps simultaneously, i.e. associating or the Compound I of using separately and at least a plant pathogenic fungi to wide region among Compound I I, III and the IV have significant activity, and described fungi especially is selected from Ascomycetes (Ascomycetes), Basidiomycetes (Basidiomycetes), Phycomycetes (Phycomycetes) and deuteromycetes (Deuteromycetes) fungi.In them some play systemic action and therefore also can be used as blade face and soil effect fungicide.
They are even more important to a large amount of fungies of control in various crops such as cotton, vegetable variety (for example cucumber, beans, tomato, potato and cucurbitaceous plant), barley, dogstail, oat, banana, coffee, corn, fruit variety, rice, rye, soybean, grape vine, wheat, ornamental plants, sugarcane and various seed.
They are particularly suitable for preventing and treating the following plants pathogenic epiphyte: the standing grain powdery mildew in the cereal class (Blumeria graminis) (powdery mildew), two spore powdery mildews (Erysiphecichoracearum) in the cucurbitaceous plant and monofilament shell (Sphaerotheca fuliginea), apple mildew bacterium in the apple (Podosphaera leucotricha), grape snag shell (Uncinula necator) in the grape vine, handle rest fungus (Puccinia) in the cereal class belongs to, cotton, rhizoctonia in rice and the lawn (Rhizoctonia) belongs to, smut in cereal class and the sugarcane (Ustilago) belongs to, venturia inaequalis in the apple (Venturiainaequalis) (scab), length in the cereal class spore (Helminthosporium) of wriggling belongs to, wheat glume blight bacterium (Septoria nodorum) in the wheat, strawberry, vegetables, Botrytis cinerea in ornamental plants and the grape vine (Botrytis cinerea) (gray mold), peanut tail spore (Cercosporaarachidicola) in the peanut, eye spot bacterium (Pseudocercosporellaherpotrichoides) in wheat and the barley, Pyricularia oryzae in the rice (Pyricularia oryzae), phytophthora infestans in potato and the tomato (Phytophthora infestans), grape in the grape vine is given birth to single shaft mould (Plasmoparaviticola), false downy mildew (Pseudoperonospora) in lupulus and the cucumber belongs to, chain lattice spore (Alternaria) in vegetables and the fruit belongs to, and the ball chamber bacterium (Mycosphaerella) in the banana belongs to and Neurospora (Fusarium) and wheel branch spore (Verticillium) genus.
In addition, they can also be used for protective material (for example protecting timber) and not be subjected to the infringement of Paecilomyces varioti (Paecilomyces variotii) for example to make it.
At least a can promptly using together or separately, or use successively simultaneously among Compound I and Compound I I, III and the IV, the order under using separately is usually to preventing and treating the result without any influence.
Compound I and II are usually with 20: 1 to 1: 20, and especially 10: 1 to 1: 10, preferred 5: 1 to 1: 5 weight ratio was used.
Compound I and III are usually with 20: 1 to 1: 20, and especially 10: 1 to 1: 10, preferred 5: 1 to 1: 5 weight ratio was used.
Compound I and IV are usually with 20: 1 to 1: 20, and especially 10: 1 to 1: 10, preferred 5: 1 to 1: 5 weight ratio was used.
The kind that depends on required effect, the rate of application of mixture of the present invention are 0.01-8kg/ha in the crops zone especially, preferred 0.1-5kg/ha, especially 0.1-3.0kg/ha.
The rate of application of Compound I is 0.01-1kg/ha, preferred 0.05-0.5kg/ha, especially 0.05-0.3kg/ha.
Correspondingly, the rate of application of Compound I I is 0.01-1kg/ha, preferred 0.02-0.5kg/ha, especially 0.05-0.3kg/ha.
Correspondingly, the rate of application of compound III is 0.01-1kg/ha, preferred 0.02-0.5kg/ha, especially 0.05-0.3kg/ha.
Correspondingly, the rate of application of compound IV is 0.01-1kg/ha, preferred 0.02-0.5kg/ha, especially 0.05-0.3kg/ha.
For seed treatment, the rate of application of this mixture is generally the 0.001-250g/kg seed, preferred 0.01-100g/kg seed, especially 0.01-50g/kg seed.
If will prevent and treat the plant-pathogenic harmful fungoid, then at least a independent or co-administered or Compound I among Compound I and Compound I I, III and the IV and at least a mixture among Compound I I, III or the IV uses by before or after the plant seeding or before or after plant emerges seed, plant or soil spraying or dusting being carried out.
At least a water-based, oiliness or other suspension that promptly sprays solution, powder and form of suspension or highly concentrate that for example can be mixed with among Fungicidal synergistic mixtures of the present invention or Compound I and Compound I I, III and the IV, dispersion, emulsion, oil dispersion, stick with paste, pulvis broadcasts sowing the form with material or granula, and can be by spraying, atomizing, dusting, broadcast sowing or water and use.Type of service depends on the purpose that is intended to; Under any circumstance all should guarantee the meticulous as far as possible and distribution equably of mixture of the present invention.
Preparaton prepares by known mode own, for example prepares by adding solvent and/or carrier.Usually inert additwe such as emulsifier or dispersant are mixed with preparaton.
Suitable surfactant be aromatic sulfonic acid such as lignin-, phenol-, naphthalene-and the alkali metal salt of dibutyl naphthalene sulfonic acids and fatty acid, alkali salt and ammonium salt, alkyl-and alkylaryl sulfonates, alkyl, lauryl ether and aliphatic alcohol sulfate and sulphation 16-, 17-and the salt of octadecanol or fatty alcohol glycol ether, the condensation product of sulfonated naphthalene and derivative thereof and formaldehyde, the condensation product of naphthalene or naphthalene sulfonic acids and phenol and formaldehyde, polyoxyethylene octylphenol ether, the ethoxylation iso-octyl-, octyl group-or nonyl phenol, alkyl phenol or tributyl phenyl polyglycol ether, alkyl aryl polyether alcohol, different tridecanol, fatty alcohol/ethylene oxide condensation product, ethoxylated castor oil, polyoxyethylene alkyl ether or polyoxypropylene, laruyl alcohol polyglycol ether acetic acid esters, sorbitol ester, lignin sulfite waste liquor or methylcellulose.
Powder, broadcast sowing with material and pulvis and can prepare by at least a mixture of at least a or Compound I in Compound I I, III or IV among Compound I and Compound I I, III or the IV mixed or grind with solid carrier.
Granula (for example coating granula, dipping granula or homogeneous phase granula) is usually by preparing reactive compound and solid carrier adhesion.
Filler or solid carrier for example are that ore deposit soil is as silica, silica gel, silicate, talcum, kaolin, lime stone, lime, chalk, bole, loess, clay, dolomite, diatomite, calcium sulphate, magnesium sulfate, magnesia; The synthetic material that grinds; Fertilizer such as ammonium sulfate, ammonium phosphate, ammonium nitrate, urea; The product of plant origin such as flour, bark powder, wood powder and shuck powder; Cellulose powder or other solid carrier.
Preparaton comprises 0.1-95 weight % usually, at least a mixture among at least a or Compound I and Compound I I, III or the IV among the Compound I of preferred 0.5-90 weight % and Compound I I, III or the IV.Reactive compound is with 90-100%, and the purity % (according to NMR spectrum or HPLC) of preferred 95-100 uses.
Compound I, II, III and IV, mixture or corresponding preparaton are by using with at least a processing harmful fungoid among Compound I and Compound I I, III or the IV, its plant, seed, soil, zone, material or space of dwelling the dried rhizome of rehmannia or wanting to prevent and treat them with the mixture of antifungal effective dose or under situation about using separately.
Use and before or after harmful fungoid infects, to carry out.
Application Example
The Synergistic active of mixture of the present invention confirms by following test:
Reactive compound is mixed with 10% emulsion separately or together in the mixture of 63 weight % cyclohexanone and 27 weight % emulsifier, and is diluted with water to desired concn.
Infect percentage evaluation by measuring leaf area.Convert these percentages to effectiveness.Use the Abbot formula by following calculating render a service ( W):
W＝(1-α/β)·100
α corresponding to the fungal infection percentage of handling plant and
β is corresponding to the fungal infection percentage of (contrast) plant of being untreated.
Effectiveness is that the infect level of the level that infects of plant corresponding to the untreated control plant handled in 0 expression; Effectiveness is that 100 expression processing plants are infected.
The expection of the mixture of reactive compound is renderd a service and is used Colby formula [R.S.Colby, Weeds (weeds) 15, 20-22 (1967)] determine and with the effectiveness that observes relatively.
Colby formula: E=x+y-xy/100
E is that the expection of working concentration when being respectively the mixture of the reactive compound A of a and b and B renderd a service,
Represent with % with respect to untreated control,
X is the effectiveness of reactive compound A when using with concentration a, represents with % with respect to untreated control,
Y is the effectiveness of reactive compound B when using with concentration b, represents with the % with respect to untreated control.
Application Example 1: to the protection activity of the powdery mildew of cucumber that causes by monofilament shell (Sphaerotheca fuliginea)
Cultivar is sprayed to the drip point for " Chinese Snake " and the leaf that is in the potted plant cucumber rice shoot in cotyledon stage with the aqueous suspension with following activity compound concentration.Described suspension or emulsion are by the stock solution preparation of 10% reactive compound in the mixture of 70% cyclohexanone, 20% wetting agent and 10% emulsifier.Behind dry 20 hours of the spray-painting, with the moisture spore suspension inoculation of plant with powdery mildew of cucumber bacterium (Sphaerotheca fuliginea).Then with test plant cultivation 7 days in the 20-24 ℃ of greenhouse with the relative atmospheric humidity of 60-80%.The % naked eyes that infect with the cotyledon area are determined the powdery mildew development degree.
The visual value that will infect the percentage of leaf area converts the effectiveness of representing with the % with respect to untreated control to.Effectiveness is that to infect degree identical with untreated control in 0 expression; Effectiveness is that 100 expressions 0% are infected.The aforementioned Colby formula of expection effectiveness use of reactive compound combination is determined and is compared with the effectiveness that observes.
Table 1
Reactive compound The concentration of reactive compound in spray liquid, ppm Render a service, with respect to the % of untreated control
Contrast (being untreated) (84% infects) 0
Compound I=Prothioconazole 0.25 0.06 0.015 5 0 0
The sharp strength spy of Compound I I= 1 0.25 0.06 0.015 0 0 0 0
Compound III=chlopyrifos 0.25 0.06 0.015 0 0 0
Compound IV=thiophene worm piperazine 4 1 0.25 0.06 0.015 0 0 0 0 0
Table 2
Combination of the present invention The effectiveness that observes The effectiveness of calculating *)
The special 0.015+0.25ppm mixture of the sharp strength of Compound I=Prothioconazole+ Compound I I=1: 16 17 0
The special 0.25+1ppm mixture of the sharp strength of Compound I=Prothioconazole+ Compound I I=1: 4 64 5
The special 0.25+0.06ppm mixture of the sharp strength of Compound I=Prothioconazole+ Compound I I=4: 1 29 5
The special 0.25+0.015ppm mixture of the sharp strength of Compound I=Prothioconazole+ Compound I I=16: 1 64 5
Compound I=Prothioconazole+ compound III=chlopyrifos 0.015+0.25ppm mixture 1: 16 17 0
Compound I=Prothioconazole+ compound III=chlopyrifos 0.06+0.25ppm mixture 1: 4 29 0
Compound I=Prothioconazole+ compound III=chlopyrifos 0.25+0.06ppm mixture 4: 1 29 5
Compound I=Prothioconazole+ compound III=chlopyrifos 0.25+0.015ppm mixture 16: 1 17 5
Compound I=Prothioconazole+ compound IV=thiophene worm piperazine 0.25+4ppm mixture 1: 16 29 5
Compound I=Prothioconazole+ compound IV=thiophene worm piperazine 76 5
0.25+1ppm mixture 1: 4
Compound I=Prothioconazole+ compound IV=thiophene worm piperazine 0.06+0.25ppm mixture 1: 4 82 0
Compound I=Prothioconazole+ compound IV=thiophene worm piperazine 0.25+0.06ppm mixture 4: 1 29 5
Compound I=Prothioconazole+ compound IV=thiophene worm piperazine 0.25+0.015ppm mixture 16: 1 17 5
*) effectiveness of using the Colby formula to calculate
Result of the test shows that the effectiveness that observes is higher than the effectiveness (from Synerg 173.XLS) that prior use Colby formula calculates under all mixing ratios.

Claims (9)

1. Fungicidal mixture comprises the following component of cooperative effective quantity:
(1) 2-[2-of formula I (1-chlorine cyclopropyl)-3-(2-chlorphenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazole-3-thioketones (Prothioconazole) or its salt or adduct:
Figure A038054290002C1
Be selected from following insecticide with at least a:
(2) the sharp strength spy of formula II:
Figure A038054290002C2
Or
(3) chlopyrifos of formula III:
Figure A038054290002C3
Or
(4) the thiophene worm piperazine of formula IV:
2. as the desired Fungicidal mixture of claim 1, comprise the Prothioconazole of formula I and the sharp strength spy of formula II.
3. as the desired Fungicidal mixture of claim 1, comprise the chlopyrifos of Prothioconazole and the formula III of formula I.
4. as the desired Fungicidal mixture of claim 1, comprise the Prothioconazole of formula I and the thiophene worm piperazine of formula IV.
5. as the desired Fungicidal mixture of claim 1, the Prothioconazole-of its Chinese style I and the sharp strength spy's of formula II weight ratio is 20: 1 to 1: 20,-with the weight ratio of the chlopyrifos of formula III be that the weight ratio of the thiophene worm piperazine of 20: 1 to 1: 20 and-and formula IV is 20: 1 to 1: 20.
6. a methods for fighting harmful mushrooms comprises with the plant, seed, soil, zone, material or the space that maybe need to prevent and treat them as the desired Fungicidal mixture processing of claim 1 harmful fungoid, its habitat.
7. as the desired method of claim 6,, promptly together or separately, or use successively wherein with at least a while in formula I compound as claimed in claim 1 and formula II as claimed in claim 1, III or the IV compound.
8. as claim 6 or 7 desired methods, wherein use at least a as in the desired Fungicidal mixture of claim 1 or formula I compound and formula II, III or the IV compound with the amount of 0.01-8kg/ha.
9. a Fungicidal composition comprises as the desired Fungicidal mixture of claim 1 and solid or liquid-carrier.
CNB038054299A 2002-03-08 2003-03-04 Fungicidal mixtures based on prothioconazole and containing an insecticide Expired - Fee Related CN100393214C (en)

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Publication number Priority date Publication date Assignee Title
CN103338640A (en) * 2011-01-28 2013-10-02 迪帕克·普兰吉万达斯·沙阿 Pesticidal composition comprising sulphur, a fungicide and an agrochemical excipient

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7375059B2 (en) * 2002-03-08 2008-05-20 Basf Aktiengesellschaft Fungicidal mixtures based on prothioconazole and containing an insecticide
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US20090227799A1 (en) * 2004-08-09 2009-09-10 Kazutaka Nakamoto Novel Antimalarial Agent Containing Heterocyclic Compound
US7829585B2 (en) * 2005-03-30 2010-11-09 Eisai R&D Management Co., Ltd. Antifungal agent containing pyridine derivative
TWI385169B (en) 2005-10-31 2013-02-11 Eisai R&D Man Co Ltd Heterocyclic substituted pyridine derivatives and antifungal agent containing same
JP5376805B2 (en) * 2005-11-04 2013-12-25 日本碍子株式会社 Honeycomb structure and honeycomb catalyst body
CN1330240C (en) * 2006-03-23 2007-08-08 浙江新安化工集团股份有限公司 Pest killing composition
WO2008035726A1 (en) 2006-09-21 2008-03-27 Eisai R & D Management Co., Ltd. Pyridine derivative substituted by heteroaryl ring, and antifungal agent comprising the same
CL2007003747A1 (en) * 2006-12-22 2008-07-18 Bayer Cropscience Ag PESTICIDE COMPOSITION INCLUDING FOSETIL-AL AND AN INSECTICIDE COMPOUND; AND METHOD FOR CONTROLLING FITOPATOGEN FUNDS OR DANIN INSECTICIDES OF THE PLANTS, CROPS OR SEEDS THAT INCLUDE APPLYING SUCH COMPOSITION.
BR122019020360B1 (en) 2007-02-06 2020-08-18 Basf Se mixtures, pesticide composition, method to control harmful phytopathogenic fungi, method to protect plants from attack or infestation by insects, mites or nematodes and method to protect seed
CA2676422C (en) 2007-02-06 2018-10-16 Lixte Biotechnology Holdings, Inc. Oxabicycloheptanes and oxabicycloheptenes, their preparation and use
AU2008244436B2 (en) 2007-04-25 2013-03-14 Basf Se Fungicide mixtures
CA2685194A1 (en) * 2007-04-27 2008-11-13 Eisai R&D Management Co., Ltd. Heterocycle-substituted pyridine derivatives salt or crystal thereof
TW200841879A (en) * 2007-04-27 2008-11-01 Eisai R&D Man Co Ltd Pyridine derivatives substituted by heterocyclic ring and phosphonoamino group, and anti-fungal agent containing same
MX2010003417A (en) 2007-10-01 2010-09-10 Lixte Biotechnology Inc Hdac inhibitors.
US8513287B2 (en) 2007-12-27 2013-08-20 Eisai R&D Management Co., Ltd. Heterocyclic ring and phosphonoxymethyl group substituted pyridine derivatives and antifungal agent containing same
AR071642A1 (en) * 2008-02-05 2010-07-07 Basf Se PESTICIDE MIXTURES
EP2242370A2 (en) * 2008-02-05 2010-10-27 Basf Se Pesticidal mixtures
US20110092466A1 (en) * 2008-05-08 2011-04-21 Basf Se Method for Protecting Soybeans from Being Infected by Fungi
CN103250712A (en) 2008-07-04 2013-08-21 巴斯夫欧洲公司 Fungicidal mixtures comprising substituted 1-methylpyrazol-4-ylcarboxanilides
WO2010147612A1 (en) 2009-06-18 2010-12-23 Lixte Biotechnology, Inc. Methods of modulating cell regulation by inhibiting p53
US8227473B2 (en) 2008-08-01 2012-07-24 Lixte Biotechnology, Inc. Oxabicycloheptanes and oxabicycloheptenes, their preparation and use
US8188119B2 (en) 2008-10-24 2012-05-29 Eisai R&D Management Co., Ltd Pyridine derivatives substituted with heterocyclic ring and γ-glutamylamino group, and antifungal agents containing same
CN104430378A (en) * 2009-07-16 2015-03-25 拜尔农作物科学股份公司 Synergistic active substance combinations containing phenyl triazoles
EP2484210A1 (en) 2011-02-08 2012-08-08 Basf Se Pesticidal compositions
JP2016516772A (en) 2013-04-09 2016-06-09 リクスト・バイオテクノロジー，インコーポレイテッド Formulation of oxacycloheptane and oxabicycloheptene
CN103461362B (en) * 2013-09-05 2014-12-24 江苏龙灯化学有限公司 Sterilizing active ingredient composition
WO2016034353A1 (en) * 2014-09-03 2016-03-10 Basf Se Pesticidally active mixtures
CN104322558B (en) * 2014-09-30 2017-04-26 四川利尔作物科学有限公司 Sterilization composition and applications thereof
CN107535518A (en) * 2016-06-28 2018-01-05 四川利尔作物科学有限公司 Seed treatment composition and its application
CN107549190A (en) * 2016-07-01 2018-01-09 四川利尔作物科学有限公司 Seed treatment composition and its application
CN107788009A (en) * 2016-08-29 2018-03-13 四川利尔作物科学有限公司 Seed treatment composition and its application

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL292088A (en) 1962-04-30 1900-01-01
AU5042585A (en) * 1984-12-10 1986-07-17 Dow Chemical Company, The Wood fungicides containing chlorpyrifos
DE3641554C2 (en) * 1986-12-05 1995-04-06 Solvay Werke Gmbh Wood preservatives
TW240163B (en) 1992-07-22 1995-02-11 Syngenta Participations Ag Oxadiazine derivatives
US6022871A (en) 1992-07-22 2000-02-08 Novartis Corporation Oxadiazine derivatives
BR9407120A (en) * 1993-06-21 1996-09-03 Bayer Ag Combinations of fungicidal active substances
FR2712144B1 (en) * 1993-11-04 1997-07-18 Rhone Poulenc Agrochimie Association of a fungicide with an azole group with an insecticide with a pyrazole, pyrrole or phenylimidazole group.
DE19528046A1 (en) * 1994-11-21 1996-05-23 Bayer Ag New sulphur substd tri:azole derivs
EP0883345A1 (en) * 1995-12-18 1998-12-16 Novartis AG Pesticidal composition
DE19548873A1 (en) * 1995-12-27 1997-07-03 Bayer Ag Stable, synergistic, broad-spectrum wood preservative composition
JP3810480B2 (en) * 1996-05-30 2006-08-16 バイエルクロップサイエンス株式会社 Bactericidal insecticidal composition
DE19716257A1 (en) 1997-04-18 1998-10-22 Bayer Ag Fungicidal active ingredient combination
CA2311796A1 (en) * 1997-11-28 1999-06-10 Peter M. Pugliese Zwitterionic fatty acid compounds for anti-inflammation
CN1186602A (en) * 1998-01-19 1998-07-08 成都华西农药厂 Recompounded incecticide of chlorpyrifos and pyrethrin
WO1999048368A1 (en) 1998-03-24 1999-09-30 Basf Aktiengesellschaft Fungicide mixtures based on triple oxime ether derivatives and rice fungicides
BR9909048A (en) * 1998-03-24 2000-12-05 Basf Ag Mixture for crop protection, process to control harmful fungi
DE19829075A1 (en) * 1998-06-17 1999-12-23 Bayer Ag Means for controlling plant pests
DE19948590A1 (en) * 1999-10-08 2001-04-12 Bayer Ag Synergistic fungicidal and acaricidal composition, especially useful for plant protection, contains cyclic ketoenol and other active agent(s), e.g. fluquinconazole, maneb, captan, sulfur or copper
DE19956098A1 (en) * 1999-11-22 2001-05-23 Bayer Ag Synergistic plant fungicide composition containing spiroxamine, quinoxyfen and imidacloprid, thiacloprid and/or thiamethoxam, especially effective against cereal diseases
WO2003027099A1 (en) * 2001-09-21 2003-04-03 E. I. Du Pont De Nemours And Company Arthropodicidal anthranilamides
US7375059B2 (en) * 2002-03-08 2008-05-20 Basf Aktiengesellschaft Fungicidal mixtures based on prothioconazole and containing an insecticide

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103338640A (en) * 2011-01-28 2013-10-02 迪帕克·普兰吉万达斯·沙阿 Pesticidal composition comprising sulphur, a fungicide and an agrochemical excipient

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